Clearly Better by Intercom Alcohol-Free Hand Sanitizer

Clearly Better by Intercom Alcohol-Free Hand Sanitizer by

Drug Labeling and Warnings

Clearly Better by Intercom Alcohol-Free Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Dyno Manufacturing. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CLEARLY BETTER BY INTERCOM ALCOHOL-FREE HAND SANITIZER- benzalkonium chloride 0.1% liquid 
Dyno Manufacturing

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Clearly Better by Intercom Alcohol-Free Hand Sanitizer

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Uses

  • For hand washing to help reduce bacteria on the skin
  • For use when soap is not available

Warnings

For external use only.

When using this product

Avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor

if irritation or redness develops, or if condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Pump a small amount of foam into palm of hand
  • Rub thoroughly over all surfaces of both hands
  • Rub hands together briskly until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive Ingredients

Water, Cocamidopropyl PG-Dimonium Chloride Phosphate, dihyrdroxyethyl cocamine oxide, acetamidoethoxyethanol, citric acid, Fragrance

Clearly Better by Intercom Alcohol-Free Hand Sanitizer

labellabel

CLEARLY BETTER BY INTERCOM ALCOHOL-FREE HAND SANITIZER 
benzalkonium chloride 0.1% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 79532-013
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE10 g  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
WATER (UNII: 059QF0KO0R)  
ACETAMIDOETHOXYETHANOL (UNII: LVX2APC4XR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 79532-013-341000 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/01/2021
Labeler - Dyno Manufacturing (015718256)

Revised: 3/2021
 

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.